The web user interface supports collaboration among various departments or geographic locations.
READY! medicinal Product database configuration is a web-based, innovative Regulatory Information Management system (RIMS) that handles your organisation’s critical data as a single reference source.
Using READY! is simple and users like it.
READY! is based on ISO IDMP standards and SPOR controlled vocabularies. It can be easily configured to meet your specific company requirements.
Our regulatory database configuration enables efficient planning, tracking, and monitoring of activities and tasks across various departments.
Automatic reminders and email alerts ensure that users remain focused on their daily work and never miss deadlines.
READY! serves as a comprehensive replacement for the multitude of Excel spreadsheets commonly used throughout your company.
READY! for ePI
Prepare, submit, and maintain documents in ePI with our pre-configured READY! platform.
Product information, Labelling
Increase efficiency in the approval of PI during regulatory procedures.
Regulatory Affairs
Replace Excel spreadsheets, shared drives, and outdated regulatory databases.
Article 57 reporting gateway
Exchange medicinal product information with a click on one button.
Pharmacovigilance
Promote, maintain, and improve compliance with the legal requirements.
Development
Track milestones and store documents created in the development of a new medicine.
Quality Assurance
Manage processes, documents, and products in one integrated platform.
Are you READY! ?
Manage product information, safety data, and documents in one validated environment.
READY! is based around the idea that companies need updated, current information about their products in all of their iterations.
It has been meticulously developed to address the unique requirements of managing both structured (IDMP medicinal product information) and unstructured data (documents, forms, records) within the pharmaceutical industry.
